1 ipients developed a widespread, progressive, violaceous, and hyperkeratotic skin eruption.

2                                              Violaceous bullae, hypotension, fever, and evidence of o

3 nth history of numbness, tingling, and faint violaceous discoloration of the tips of multiple fingers

4  Clinically, the lesions presented as red or violaceous (lichenoid) cutaneous maculopapules.

5 ecipients who developed characteristic pink, violaceous, or brown hyperkeratotic papules and plaques

6 ease characterized by pruritic, flat-topped, violaceous papules on the skin.

7 HSCT, namely finger pad inflammation, palmar violaceous papules, and digital ulcerations.

8 HSCT, namely finger pad inflammation, palmar violaceous papules, and digital ulcerations.

9      Smooth, indurated, nonscarring, pink to violaceous papules, plaques, or nodules, devoid of surfa

10 atosis skin lesions, including tender red or violaceous papules, sometimes edematous, without fever,

11 ant cutaneous disease that manifested as red violaceous plaques of the cheeks, nose, ears, fingers, a

12 sive atrophy in the past 3 months, erythema, violaceous rim or color, warmth to the touch, induration

13 cification and occlusion/thrombosis leads to violaceous skin lesions, which progress to nonhealing ul

14 : (i) presence of ulcer(s) with erythematous/violaceous undermining wound borders, (ii) presence of a